FDA 510(k), K883665, COONRAD III TOTAL ELBOW
FDA 510(k), K883665, COONRAD III TOTAL ELBOW
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510(K) Number: K883665
Device Name: COONRAD III TOTAL ELBOW
Manufacturer:
Device Classification Name: Prosthesis, Elbow, Constrained, Cemented
Regulation Number: 888.3150
Classification Product Code: JDC
Date Received: 08/26/1988
Decision Date: 02/03/1989
Regulation Medical Specialty: Orthopedic
Device Name: COONRAD III TOTAL ELBOW
Manufacturer:
Device Classification Name: Prosthesis, Elbow, Constrained, Cemented
Regulation Number: 888.3150
Classification Product Code: JDC
Date Received: 08/26/1988
Decision Date: 02/03/1989
Regulation Medical Specialty: Orthopedic